PIU CHE DOLCI INC. Recall: Due to potential Salmonella contamination

🇺🇸 United States

1. January 17, 2025 - Recall initiated
2. February 19, 2025 - Reported by source
3. April 18, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0551-2025

Event ID

96217

Status

Terminated

Classification

Class I

Company

PIU CHE DOLCI INC.

Product description

Sweet Cream Mini Patisseries, 30 piece variety tray of mini pastries, Net Wt 1 kg, 4 trays per master carton, total Net wt 8.8 lbs, Keep Frozen, All best before dates from 2025/06/17 up to and including 2025/11/15.

Quantity

1,923 master cartons in total (403 master cartons in the US)

Reason

Due to potential Salmonella contamination

Recall initiation date

January 17, 2025

Report date

February 19, 2025

Classification date

Not published in this source record

Termination date

April 18, 2025

Distribution pattern

Distributed in the states of NJ and FL.

UPC, lot, and code information

SHIP DATE LOTE # EXP DATE SEP 12 2024 24200 JUL-18-2025 SEP 12 2024 24204 JUL-22-2025 SEP 12 2024 24201 JUL-19-2025 SEP 12 2024 24199 JUL-17-2025 SEP 12 2024 24204 JUL-22-2025 SEP 12 2024 24176 JUN-24-2025 SEP 12 2024 24177 JUN-25-2025 SEP 12 2024 24180 JUN-28-2025 OCT 09 2024 24190 JUL-08-2025

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: PIU CHE DOLCI INC.

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
New Jersey	1
Florida	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

• Email
• X / Twitter
• Facebook